1. www.rtog.org 1 MARCH 2012 Regulatory Documents & the CTSU

2. www.rtog.org 2 Disclaimer The following presentation is being given for RTOG studies only. The information represented here while current may change due to changes within RTOG internal processes or because of federal regulatory guidelines. Therefore, you may not reproduce or distribute any of the presentation without obtaining RTOG’s prior written consent.

3. www.rtog.org 3 Regulatory Documents All regulatory documents for US, Canadian & Non North American sites are submitted to the CTSU for cataloguing and data entry –Continuing Reviews –Approvals of amendments –IRB initial study approvals –IRB approved consent forms (translation required for Non English speaking countries/provinces)

4. www.rtog.org 4 Continuing IRB Approval IRB approval must continue untilIRB approval must continue until Finite StudiesFinite Studies –All subjects accrued have completed treatment and follow up Non Finite StudiesNon Finite Studies –All subjects are deceased Additional requirements for both finite & non finite studiesAdditional requirements for both finite & non finite studies –No further accrual is anticipated –All data forms have been submitted –All queries to date have been resolved –RTOG approves the site for early closure (see form) IRB approval remains necessary, even after RTOG study closure and until RTOG termination unless all the above criteria/requirements have been metIRB approval remains necessary, even after RTOG study closure and until RTOG termination unless all the above criteria/requirements have been met Only RTOG can classify a study as "terminated" (Database locked)Only RTOG can classify a study as "terminated" (Database locked) Notification of Study Termination will be received via broadcastNotification of Study Termination will be received via broadcast A formal request is required for early closure when all criteria metA formal request is required for early closure when all criteria met

5. www.rtog.org 5 Form to Request Early IRB Closure http://www.rtog.org/ResearchAssociates/RegulatoryInformation/EarlyIRBClosure.aspx http://www.rtog.org/ResearchAssociates/RegulatoryInformation/EarlyIRBClosure.aspx

6. www.rtog.org 6 Requests for Early IRB Closure Request form must be submitted to and approved by RTOGRequest form must be submitted to and approved by RTOG The Form has Multiple purposesThe Form has Multiple purposes –Request consideration for early closure with IRB –Request closure with IRB when no patients enrolled on study –Transfer IRB responsibilities RTOG response with approval of the request is required prior to taking any closure actionRTOG response with approval of the request is required prior to taking any closure action Internal multi department review at RTOG HQ can take 7-10 business days to completeInternal multi department review at RTOG HQ can take 7-10 business days to complete Sites will still be required to respond to queries even after study closure with the IRBSites will still be required to respond to queries even after study closure with the IRB

7. www.rtog.org 7 Continuing IRB Approval IMPORTANT NOTE Full member institutions that have affiliates that use the Full Member IRB as their IRB of record must ensure that those affiliate/ Joint Center institutions had also never put any patients on studies they are considering closing with the IRB. If they have, then the main IRB must keep this study open for annual review.IMPORTANT NOTE Full member institutions that have affiliates that use the Full Member IRB as their IRB of record must ensure that those affiliate/ Joint Center institutions had also never put any patients on studies they are considering closing with the IRB. If they have, then the main IRB must keep this study open for annual review.

8. www.rtog.org 8 Special Handling Handling of all other study specific regulatory documentation is detailed in Sections 5.0 or 7.0 of the protocolHandling of all other study specific regulatory documentation is detailed in Sections 5.0 or 7.0 of the protocol Study Agent Shipment Form (SASF) Sponsor required documentation Questionnaires Training Certifications RT Certifications Non English speaking Canadian & Non North American sites are required to supply the Certified/Verified English translation and native language copy of the IC with their regulatory approvalsNon English speaking Canadian & Non North American sites are required to supply the Certified/Verified English translation and native language copy of the IC with their regulatory approvals Other special procedures may exist for Non North American sitesOther special procedures may exist for Non North American sites

9. www.rtog.org 9 Correlative Components Each participating institution must be prepared to participate in all correlative components/have a plan in place to facilitate participation and must offer every patient the opportunity to participate in these components.Each participating institution must be prepared to participate in all correlative components/have a plan in place to facilitate participation and must offer every patient the opportunity to participate in these components. ONLY THE PATIENT can decline to participate in the correlative components of a studyONLY THE PATIENT can decline to participate in the correlative components of a study The majority of RTOG studies require varying degrees of specimen collection as part of eligibility, stratification or protocol treatment.The majority of RTOG studies require varying degrees of specimen collection as part of eligibility, stratification or protocol treatment. Sites are encouraged to become more organized in their efforts and coordinate tissue banking collections with other protocol required specimen collections whenever possible.Sites are encouraged to become more organized in their efforts and coordinate tissue banking collections with other protocol required specimen collections whenever possible. In the event tissue is collected/residing at another facility RTOG expects a good faith effort to obtain the retrospective specimens but the site will not be penalized if it is not possible.In the event tissue is collected/residing at another facility RTOG expects a good faith effort to obtain the retrospective specimens but the site will not be penalized if it is not possible. Prospectively the site must inform the collecting entity that future specimens collected are expected to be forwarded along with the appropriate submission form for tissue banking as noted in the protocol.Prospectively the site must inform the collecting entity that future specimens collected are expected to be forwarded along with the appropriate submission form for tissue banking as noted in the protocol.

10. www.rtog.org 10 CTSU Forms & Guidance Can be found on the RTOG website www.rtog.org www.rtog.org under RA/Regulatory Info/CTSU Filing Requirements –IRB Certification Forms –310 Certification Form –IRB Transmittal Forms –Guidance for completing the forms –RSS Flow sheet NCI Required Forms are also available here –FDA 1572 –CTEP Supplemental Investigator Data Form (IDF) –CTEP Financial Disclosure

11. www.rtog.org 11 Proper Labeling Ensures Proper Processing Please identify all information submitted to the CTSU with the institution’s NCI Code on the transmittal/certification formPlease identify all information submitted to the CTSU with the institution’s NCI Code on the transmittal/certification form If the submission covers more than one institution or an entire CCOP all assigned individual NCI institution codes covered under the approval must be listed on the transmittal/certification form or supplemental pageIf the submission covers more than one institution or an entire CCOP all assigned individual NCI institution codes covered under the approval must be listed on the transmittal/certification form or supplemental page

12. www.rtog.org 12 CTSU Forms Transmittal/Certification

13. www.rtog.org 13 Resolving Regulatory Issues All issues for U.S., Canadian and Non North American sites with submitted regulatory documents should be handled directly through the CTSU.All issues for U.S., Canadian and Non North American sites with submitted regulatory documents should be handled directly through the CTSU. RTOG does not have access to copies of regulatory documents that have been submitted to the CTSU.

14. www.rtog.org 14 Checking Registration Status Visit the CTSU Website: https://www.ctsu.org/public/ https://www.ctsu.org/public/ Requires a CTSU username & passwordRequires a CTSU username & password Sites are identified by NCI CodeSites are identified by NCI Code Lists all requirements for studyLists all requirements for study Lists items not in complianceLists items not in compliance Now available for Non North American sitesNow available for Non North American sites

15. www.rtog.org 15 To obtain a CTSU password…

16. www.rtog.org 16 Points of Contact for the CTSU Help Desk: 1-888-823-5923Help Desk: 1-888-823-5923 Regulatory Help Desk: 866-651-CTSU (2878)Regulatory Help Desk: 866-651-CTSU (2878) E-mail for questions: ctsucontact@westat.comE-mail for questions: ctsucontact@westat.comctsucontact@westat.com For Regulatory Submissions: Fax Number: 215-569-0206Fax Number: 215-569-0206 E-mail : CTSURegulatory@ctsu.coccg.orgE-mail : CTSURegulatory@ctsu.coccg.org CTSURegulatory@ctsu.coccg.org Mailing Address: Mailing Address: CTSU Regulatory Office Coalition of National Cancer Cooperative Groups 1818 Market Street, Suite 1100 Philadelphia, PA 19103 Website: http://members.ctsu.org/Website: http://members.ctsu.org/http://members.ctsu.org/